Canonical Allele Identifier: CA2059476260
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102917279A= , CM000674.2:g.102917279A= GRCh38
NC_000012.11:g.103311057A= , CM000674.1:g.103311057A= GRCh37
NC_000012.10:g.101835187A= NCBI36
NG_008690.1:g.5324T=
NG_008690.2:g.46132T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000546708.5:n.493-54T=
ENST00000546844.1:c.-95-54T= ENSP00000446658.1:n.-95-54T=
ENST00000547319.1:n.217-54T=
ENST00000551337.5:c.-95-54T= ENSP00000447620.1:n.-95-54T=
ENST00000553106.5:c.-149T= ENSP00000448059.1:n.-149T=
ENST00000635500.1:n.29-4381T=
NM_000277.1:c.-149T= NP_000268.1:n.-149T=
NM_000277.2:c.-149T= NP_000268.1:n.-149T=
NM_001354304.1:c.-95-54T= NP_001341233.1:n.-95-54T=
NM_001354304.2:c.-95-54T= NP_001341233.1:n.-95-54T=